Diagnosis and Treatment of Children with Suspected Metabolic Disease

Pediatrics

Volumn , Issue , 2005, Pages 1866-1875

  Enns, Gregory M ^a   Steiner, Robert D ^b  

^a STANFORD UNIVERSITY   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33744935313     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-323-01199-0.50296-6     Document Type: Chapter

References (5)

1. Physician's Guide to the Laboratory Diagnosis of Metabolic Diseases 1996, Chapman & Hall, London. N. Blau, M. Duran, M.E. Blaskovics (Eds.).
2. Clarke JTR Acute metabolic illness in the newborn. A Clinical Guide to Inherited Metabolic Diseases 1996, 176-204. Cambridge University Press, New York.
3. Pass KA, Lane PA, Fernhoff PM, et al. US newborn screening system guidelines. II: Follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN). J Pediatr 2000, 137(4 suppl):S1-S46.
4. Saudubray J-M, Charpentier C Clinical phenotypes: Diagnosis/algorithms. The Metabolic and Molecular Bases of Inherited Disease 2001, 1327-1403. McGraw-Hill, New York. C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle (Eds.).
5. Steiner RD, Cederbaum SD Laboratory evaluation of urea cycle disorders. J Pediatr 2001, 138:S21-S29.